ID: ALA5089257

Max Phase: Preclinical

Molecular Formula: C25H24N4O4S2

Molecular Weight: 508.63

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CC(=O)N1CCc2c(sc3nc(SCC(=O)Nc4cccc(C)c4)n(Cc4ccco4)c(=O)c23)C1

Standard InChI:  InChI=1S/C25H24N4O4S2/c1-15-5-3-6-17(11-15)26-21(31)14-34-25-27-23-22(24(32)29(25)12-18-7-4-10-33-18)19-8-9-28(16(2)30)13-20(19)35-23/h3-7,10-11H,8-9,12-14H2,1-2H3,(H,26,31)

Standard InChI Key:  PQMQUKJGFYOHJZ-UHFFFAOYSA-N

Associated Targets(Human)

Bromodomain-containing protein 3 1086 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 508.63Molecular Weight (Monoisotopic): 508.1239AlogP: 4.04#Rotatable Bonds: 6
Polar Surface Area: 97.44Molecular Species: NEUTRALHBA: 8HBD: 1
#RO5 Violations: 1HBA (Lipinski): 8HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 13.66CX Basic pKa: 2.19CX LogP: 3.56CX LogD: 3.56
Aromatic Rings: 4Heavy Atoms: 35QED Weighted: 0.31Np Likeness Score: -2.77

References

1. Carrasco K, Montersino C, Derviaux C, Saez-Ayala M, Hoffer L, Restouin A, Castellano R, Casassa J, Roche P, Pasquier E, Combes S, Morelli X, Collette Y, Betzi S..  (2022)  CRCM5484: A BET-BDII Selective Compound with Differential Anti-leukemic Drug Modulation.,  65  (7.0): [PMID:35348328] [10.1021/acs.jmedchem.1c02168]

Source